NDC 42708-177 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC42708-177

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
QPharma Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206553
Marketed since
January 17, 2017
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
42708-177-21 sample21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)Jun 5, 2023

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